Cas 1190878-76-2,1-deoxy-1-(5-(p-methylbenzoyl)-4-(ethoxycarbonyl)-1H-1,2,3-triazol-1-yl)-2,3,5-tri-O-acetyl-β-D-ribofuranose

1190878-76-2

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Basic information

Product Name: 1-deoxy-1-(5-(p-methylbenzoyl)-4-(ethoxycarbonyl)-1H-1,2,3-triazol-1-yl)-2,3,5-tri-O-acetyl-β-D-ribofuranose
Synonyms: 1-deoxy-1-(5-(p-methylbenzoyl)-4-(ethoxycarbonyl)-1H-1,2,3-triazol-1-yl)-2,3,5-tri-O-acetyl-β-D-ribofuranose
CAS NO:1190878-76-2
Molecular Formula:
Molecular Weight: 517.492
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 1-deoxy-1-(5-(p-methylbenzoyl)-4-(ethoxycarbonyl)-1H-1,2,3-triazol-1-yl)-2,3,5-tri-O-acetyl-β-D-ribofuranose(CAS DataBase Reference)
NIST Chemistry Reference: 1-deoxy-1-(5-(p-methylbenzoyl)-4-(ethoxycarbonyl)-1H-1,2,3-triazol-1-yl)-2,3,5-tri-O-acetyl-β-D-ribofuranose(1190878-76-2)
EPA Substance Registry System: 1-deoxy-1-(5-(p-methylbenzoyl)-4-(ethoxycarbonyl)-1H-1,2,3-triazol-1-yl)-2,3,5-tri-O-acetyl-β-D-ribofuranose(1190878-76-2)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1190878-76-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1190878-76-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,0,8,7 and 8 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1190878-76:
(9*1)+(8*1)+(7*9)+(6*0)+(5*8)+(4*7)+(3*8)+(2*7)+(1*6)=192
192 % 10 = 2
So 1190878-76-2 is a valid CAS Registry Number.

1190878-76-2Upstream product

1190878-76-2Downstream Products

1190878-76-2Relevant academic research and scientific papers

Tandem azide-alkyne 1,3-dipolar cycloaddition/electrophilic addition: A concise three-component route to 4,5-disubstituted triazolyl-nucleosides

Malnuit, Vincent,Duca, Maria,Manout, Anwar,Bougrin, Khalid,Benhida, Rachid

, p. 2123 - 2128 (2009)

A one-pot, three-component approach to a new family of 4,5-functionalized triazolyl-nucleosides is described. The method relies on the one-pot azide-alkyne 1,3-cycloaddition/electrophilic addition tandem reaction, which affords good yields of the correspo

In Vitro and in Vivo Evaluation of Fully Substituted (5-(3-Ethoxy-3-oxopropynyl)-4-(ethoxycarbonyl)-1,2,3-triazolyl-glycosides as Original Nucleoside Analogues to Circumvent Resistance in Myeloid Malignancies

Amdouni, Hella,Robert, Guillaume,Driowya, Mohsine,Furstoss, Nathan,Métier, Camille,Dubois, Alix,Dufies, Maeva,Zerhouni, Marwa,Orange, Fran?ois,Lacas-Gervais, Sandra,Bougrin, Khalid,Martin, Anthony R.,Auberger, Patrick,Benhida, Rachid

, p. 1523 - 1533 (2017)

A series of nucleoside analogues bearing a 1,4,5-trisubstituted-1,2,3-triazole aglycone was synthesized using a straightforward click/electrophilic addition or click/oxidative coupling tandem procedures. SAR analysis, using cell culture assays, led to the

ACADESINE DERIVATIVES, PRODUCTS AND COMPOSITIONS INCLUDING SAME, THERAPUETIC USES THEREOF, AND METHODS FOR SYNTHESIZING SAME

-

, (2014/07/08)

Acadesine derivatives as a drug, as well as the derivatives for the treatment of cancer and in particular for the treatment of chronic myeloid leukemia are described. Also, product containing the derivatives and at least one second active ingredient as a

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